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Most Viewed
Neurological findings in incontinentia pigmenti; a review.
Spatial and temporal characteristics of gait as outcome measures in multiple sclerosis (EDSS 0 to 6.5).
Human myelin proteome and comparative analysis with mouse myelin.
High prevalence of abnormal gastrointestinal permeability in moderate-severe asthma.
[Pathology, diagnosis, and treatment of combined central and peripheral demyelination].
Fluctuating neurological symptoms in demyelinating disease mimicking an acute ischaemic stroke.
Acute demyelinating events following vaccines - a case centered analysis.
Levodopa-responsive Holmes' Tremor Caused by a Single Inflammatory Demyelinating Lesion.
Lotensin: Cheap 180
A Comparison of Magnetization Transfer Methods to Assess Brain and Cervical Cord Microstructure in Multiple Sclerosis.
Immunomodulation by vitamin D in multiple sclerosis: More than IL-17.
Lung inflammation stalls Th17 cell migration en route to the central nervous system during the development of experimental autoimmune encephalomyelitis.
Disturbed spontaneous brain-activity pattern in patients with optic neuritis using amplitude of low-frequency fluctuation: a functional magnetic resonance imaging study.
The association of HLA-DRB1 and HLA-DQB1 alleles with genetic susceptibility to multiple sclerosis in the Slovak population.
Body mass index influence interferon-beta treatment response in multiple sclerosis.
Treatment adherence in multiple sclerosis: a survey of Belgian neurologists.
Catalpol induces oligodendrocyte precursor cell-mediated remyelination in vitro.
Autoimmune hepatitis/primary biliary cirrhosis overlap syndrome and associated extrahepatic autoimmune diseases.
Microglial Physiology and Pathophysiology: Insights from Genome-wide Transcriptional Profiling.
Shifting paradigms in multiple sclerosis: from disease-specific, through population-specific toward patient-specific.
Sonographic evaluation of peripheral nerves in subtypes of Guillain-Barré syndrome.
The nod-like receptor, Nlrp12, plays an anti-inflammatory role in experimental autoimmune encephalomyelitis.
Multiple sclerosis-like diagnosis as a complication of previously treated malaria in an iron and vitamin D deficient Nigerian patient.
The role of EGFR and ErbB family related proteins in the oligodendrocyte specification in germinal niches of the adult mammalian brain.
Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease.
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